Neochild, LLC is one of 15076 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neochild, LLC - FDA 510(k) Cleared Devices
Recent clearances: SAFECHILD ENTERAL FEEDING TUBE AND ACCESSORIES AND FEEDING TUBE EXTENSION SET
1
Total
1
Cleared
0
Denied
Neochild, LLC has 1 FDA 510(k) cleared medical devices. Based in Oklahoma City, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Neochild, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neochild, LLC
1 devices